作者:Alaba M. Ogunbadeniyi、Adeboye Adejare
DOI:10.1016/s0022-1139(01)00565-6
日期:2002.3
Syntheses of several fluorinated phencyclidine (PCP) analogs are described. These compounds are being used to probe PCP binding sites on N-methyl-d-aspartate (NMDA) receptors. The compounds were prepared in good yields by Grignard reaction of appropriate fluorine substituted bromobenzene with carbonitrile intermediates. Syntheses of the known compound 1-[1-(3-fluorophenyl)cyclohexyl]piperidine, and
描述了几种氟化苯环利定(PCP)类似物的合成。这些化合物用于探测N-甲基-d-天冬氨酸(NMDA)受体上的PCP结合位点。通过适当的氟取代的溴苯与腈的中间体的格氏反应,以高收率制备化合物。已知化合物1- [1-(1-(3-氟苯基)环己基]哌啶和新型化合物1- [1-(4-氟苯基)环己基]哌啶,1- [1-(3-(氟代苯基)环己基]吡咯烷的合成报道了1- [1-(4-氟苯基)环己基]吡咯烷。